Identification of mutations in the<i>MYO9A</i>gene in patients with congenital myasthenic syndrome
Congenital myasthenic syndromes are a group of rare and genetically heterogenous disorders resulting from defects in the structure and function of the neuromuscular junction. Patients with congenital myasthenic syndrome exhibit fatigable muscle weakness with a variety of accompanying phenotypes depe...
Tallennettuna:
| Päätekijät: | , , , , , , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | englanti |
| Julkaistu: |
2016
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| Linkit: | https://doi.org/10.1093/brain/aww130 |
| Tagit: |
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